Phenotype #0000092602

Individual ID 00117368
Associated disease STL1
Phenotype details myopia, avascular sheets, scoliosis, cataract, retinal detachment, chorioretinal scars, optically empty vitreous
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 42y (42 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Mouna Barat-Houari
Database submission license No license selected
Created by Mouna Barat-Houari
Date created 2017-08-22 17:37:19 +02:00 (CEST)
Date last edited N/A

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